Hutchinson-Gilford Progeria Syndrome This stem is on the Hutchinson-Gilford Progeria Syndrome. The make-up will first designate Hutchinon-Gilford Progeria Syndrome. This paper will discuss the signs and symptoms of Hutchinson-Gilford syndrome. Finally this paper reviews the case of Hutchinson-Gilford Progeria syndrome. This paper is on the Hutchinson-Gilford Progeria Syndrome (Englert .C. 2009). Hutchinson- Gilford Progeria Syndrome is a genetic condition characterized by appearance of advance aging in sisterren (Englert .C. 2009). Ninety per centum of children with Progeria have a mutation set of genes (Englert .C. 2009). The gene is passed from a family member, roundtimes it occurs without acquire (Englert .C. 2009). It is very rargonly seen in much than one child in a family. Progeria is Greek and direction prematurely sr. (Englert .C. 2009).There are different forms of Progeria, the classic eccentric person is Hutchinson- Gilford Progeria Syndrome (Englert .C . 2009). Progeria was named after the doctors who first detect it in England (Englert .C. 2009). In 1886 it was Dr. Jonathan Hutchinson, and in 1897 it was discovered by Dr. Hastings Gilford (Englert .C. 2009). There are some(prenominal) signs and symptoms of Hutchinson-Gilford Progeria Syndrome (Englert .C. 2009).
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Some are slowed growth with below-average height and weight, hair loss, including eyelashes and eyebrows (Englert .C. 2009). Patients are born feel healthy; children with Progeria begin to display the characteristics from 18-24 months (Englert .C. 2009). The expectation of Hutchinson-Gilford Progeria Syndrome is associated with a get around lifespan (Englert .C. 2009). T he lifespan is usually 18-21years some patie! nts can resilient up to thirty years (Englert .C. 2009). The cause of death is link up to the heart or a stroke (Englert .C. 2009). There are no treatment or cures for Hutchinson - Gilford Syndrome (Englert .C. 2009). Conclusion This paper discussed Hutchinson- Gilford Progeria Syndrome. This paper first defined...If you want to get a complete essay, target it on our website:
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